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FDA 510(k)

FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS

K-Number: K031067 · 2003-07-14

Decision Date2003-07-14
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS is the device name listed in this FDA 510(k) record. The listed applicant is First Quality Hygienic, Inc.. It received FDA 510(k) clearance on 2003-07-14 under 510(k) number K031067. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS?

FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS is a medical device that received FDA 510(k) clearance on 2003-07-14. The listed applicant is First Quality Hygienic, Inc.. The 510(k) number is K031067.

When did FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS receive FDA 510(k) clearance?

FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS received FDA 510(k) clearance on 2003-07-14, under 510(k) number K031067.

Who is the listed applicant for FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS?

The FDA 510(k) record lists First Quality Hygienic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS?

The FDA product code for FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS is HEB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing First Quality Hygienic, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 10 devices →

Related Devices (Code: HEB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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